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Article: Augmenting osteoporotic bone regeneration through a hydrogel-based rejuvenating microenvironment

TitleAugmenting osteoporotic bone regeneration through a hydrogel-based rejuvenating microenvironment
Authors
KeywordsBone regeneration
Focal adhesion pathway
Osteoporotic bone defects
Rejuvenating microenvironment
Secretome
Issue Date2024
Citation
Bioactive Materials, 2024, v. 41, p. 440-454 How to Cite?
AbstractOsteoporotic bone defects pose a significant challenge for bone regeneration as they exhibit impaired healing capacity and delayed healing period. To address this issue, this study introduces a hydrogel that creates a rejuvenating microenvironment, thereby facilitating efficient bone repair during the initial two weeks following bone defect surgery. The hydrogel, named GelHFS, was created through host-guest polymerization of gelatin and acrylated β-cyclodextrin. Incorporation of the human fetal mesenchymal stem cell secretome (HFS) formed GelHFS hydrogel aimed at mimicking a rejuvenated stem cell niche. Our results demonstrated that GelHFS hydrogel promotes cell stellate spreading and osteogenic differentiation via integrin β1-induced focal adhesion pathway. Implantation of GelHFS hydrogel in an osteoporotic bone defect rat model recruited endogenous integrin β1-expressing cells and enhanced new bone formation and bone strength. Our findings reveal that GelHFS hydrogel provides a rejuvenating niche for endogenous MSCs and enhances bone regeneration in osteoporotic bone defect. These findings highlight the potential of GelHFS hydrogel as an effective therapeutic strategy for addressing challenging bone healing such as osteoporotic bone regeneration.
Persistent Identifierhttp://hdl.handle.net/10722/363650
ISSN
2023 Impact Factor: 18.0
2023 SCImago Journal Rankings: 3.466

 

DC FieldValueLanguage
dc.contributor.authorZhang, Xiaoting-
dc.contributor.authorYang, Boguang-
dc.contributor.authorFeng, Lu-
dc.contributor.authorXu, Xiayi-
dc.contributor.authorWang, Chenmin-
dc.contributor.authorLee, Yuk wai-
dc.contributor.authorWang, Ming-
dc.contributor.authorLu, Xuan-
dc.contributor.authorQin, Ling-
dc.contributor.authorLin, Sien-
dc.contributor.authorBian, Liming-
dc.contributor.authorLi, Gang-
dc.date.accessioned2025-10-10T07:48:22Z-
dc.date.available2025-10-10T07:48:22Z-
dc.date.issued2024-
dc.identifier.citationBioactive Materials, 2024, v. 41, p. 440-454-
dc.identifier.issn2452-199X-
dc.identifier.urihttp://hdl.handle.net/10722/363650-
dc.description.abstractOsteoporotic bone defects pose a significant challenge for bone regeneration as they exhibit impaired healing capacity and delayed healing period. To address this issue, this study introduces a hydrogel that creates a rejuvenating microenvironment, thereby facilitating efficient bone repair during the initial two weeks following bone defect surgery. The hydrogel, named GelHFS, was created through host-guest polymerization of gelatin and acrylated β-cyclodextrin. Incorporation of the human fetal mesenchymal stem cell secretome (HFS) formed GelHFS hydrogel aimed at mimicking a rejuvenated stem cell niche. Our results demonstrated that GelHFS hydrogel promotes cell stellate spreading and osteogenic differentiation via integrin β1-induced focal adhesion pathway. Implantation of GelHFS hydrogel in an osteoporotic bone defect rat model recruited endogenous integrin β1-expressing cells and enhanced new bone formation and bone strength. Our findings reveal that GelHFS hydrogel provides a rejuvenating niche for endogenous MSCs and enhances bone regeneration in osteoporotic bone defect. These findings highlight the potential of GelHFS hydrogel as an effective therapeutic strategy for addressing challenging bone healing such as osteoporotic bone regeneration.-
dc.languageeng-
dc.relation.ispartofBioactive Materials-
dc.subjectBone regeneration-
dc.subjectFocal adhesion pathway-
dc.subjectOsteoporotic bone defects-
dc.subjectRejuvenating microenvironment-
dc.subjectSecretome-
dc.titleAugmenting osteoporotic bone regeneration through a hydrogel-based rejuvenating microenvironment-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.bioactmat.2024.07.036-
dc.identifier.scopuseid_2-s2.0-85200247769-
dc.identifier.volume41-
dc.identifier.spage440-
dc.identifier.epage454-

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